US9458300B2ActiveUtilityPatentIndex 71
Hydrophilic, aliphatic polyurethane foams
Est. expiryOct 27, 2030(~4.3 yrs left)· nominal 20-yr term from priority
C08J 9/0066A61L 15/425C08G 2101/0083A61L 15/26C08G 18/792C08G 18/302C08G 18/283A61L 15/16C08G 18/10C08L 75/04C08G 18/8064C08G 2110/0083
71
PatentIndex Score
4
Cited by
22
References
18
Claims
Abstract
The invention relates to a method for producing hydrophilic, aliphatic polyurethane foams. The invention further relates to special compositions for producing polyurethane foams either using the method according to the invention or using the polyurethane foams obtained from the compositions according to the invention, and to the use of the polyurethane foams as a wound dressing, cosmetic item, or incontinence product.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. A process for producing a hydrophilic aliphatic polyurethane foam, which comprises providing a composition comprising
A) isocyanate-functional prepolymers obtained by reaction of
A1) low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/mol with
A2) di- to hexafunctional polyalkylene oxides having an OH number of 22.5 to 112 mg KOH/g and an ethylene oxide content of 50 to 100 mol %, based on the total amount of oxyalkylene groups present,
B) alkali metal salts of weak inorganic acids, wherein the alkali metal salts of weak inorganic acids B) are selected from the group consisting of potassium hydroxide, potassium carbonate, sodium hydroxide, sodium bicarbonate, sodium carbonate, and mixtures thereof,
C) water,
D) heterocyclic 4-ring or 6-ring oligomers of low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/mol,
E) optionally catalysts different from B),
F) optionally surfactants,
G) optionally mono- or polyhydric alcohols, and
H) hydrophilic polyisocyanates obtained by reaction of
H1) low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/ml and/or polyisocyanates obtained therefrom with an isocyanate functionality of 2 to 6, with
H2) monofunctional polyalkylene oxides having an OH number of 10 to 250 and an ethylene oxide content of 50 to 100 mol %, based on the total amount of oxyalkylene groups present,
foaming and curing the composition.
2. The process as claimed in claim 1 , wherein the alkali metal salts of weak inorganic acids B) are selected from the group consisting of sodium hydroxide, sodium bicarbonate and sodium carbonate.
3. The process as claimed in claim 1 , wherein isocyanate-functional prepolymers A) having a weight fraction of below 1.0 wt % for low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/mol, based on the prepolymer, are used.
4. The process as claimed in claim 1 , wherein the components A) to H) are used in the following amounts:
A) 100 parts by weight of isocyanate-functional prepolymers,
B) 0.01 to 5 parts by weight of alkali metal salts of weak inorganic acids,
C) 0.1 to 200 parts by weight of water,
D) up to 100 parts by weight of heterocyclic oligomers,
E) 0 to 1 part by weight of catalysts,
F) 0 to 10 parts by weight of surfactants,
G) 0 to 20 parts by weight of mono- or polyhydric alcohols, and
H) up to 60 parts by weight of hydrophilic polyisocyanates.
5. The process as claimed in claim 4 , wherein the composition comprises 10 to 100 parts by weight of heterocyclic oligomers D).
6. The process as claimed in claim 4 , wherein the composition comprises 20 to 90 parts by weight of heterocyclic oligomers D).
7. The process as claimed in claim 4 , wherein the composition comprises 20 to 80 parts by weight of heterocyclic oligomers D).
8. The process as claimed in claim 1 , wherein the low molecular weight aliphatic diisocyanates A1) are hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI) or mixtures thereof.
9. The process as claimed in claim 1 , wherein the polyalkylene oxides A2) are copolymers of ethylene oxide and propylene oxide having an ethylene oxide content, based on the total amount of oxyalkylene groups present, of 60 to 85 mol %, and started on polyols or amines.
10. The process as claimed in claim 1 , wherein the polyalkylene oxides A2) have number-average molecular weights of 3000 to 8500 g/mol.
11. The process as claimed in claim 1 , wherein the polyalkylene oxides A2) have OH functionalities of 3 to 4.
12. The process as claimed in claim 1 , wherein no catalysts E) are used.
13. A composition comprising
A) isocyanate-functional prepolymers, having a weight fraction of below 1.0 wt % for low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/mol, based on the prepolymer, obtained by reaction of
A1) low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/mol with
A2) di- to hexafunctional polyalkylene oxides having an OH number of 22.5 to 112, and an ethylene oxide content of 50 to 100 mol %, based on the total amount of oxyalkylene groups present,
B) alkali metal salts of weak inorganic acids, wherein the alkali metal salts of weak inorganic acids B) are selected from the group consisting of potassium hydroxide, potassium carbonate, sodium hydroxide, sodium bicarbonate, sodium carbonate, and mixtures thereof,
C) water,
D) heterocyclic 4-ring or 6-ring oligomers of low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/mol,
E) optionally catalysts different from B),
F) optionally surfactants,
G) optionally mono- or polyhydric alcohols, and
H) hydrophilic polyisocyanates obtained by reaction of
H1) low molecular weight aliphatic diisocyanates having a molar mass of 140 to 278 g/ml and/or polyisocyanates obtained therefrom with an isocyanate functionality of 2 to 6, with
H2) monofunctional polyalkylene oxides having an OH number of 10 to 250 and an ethylene oxide content of 50 to 100 mol %, based on the total amount of oxyalkylene groups present.
14. The composition as claimed in claim 13 , wherein component A2) are tri- to hexafunctional polyalkylene oxides having an OH number of 31.5 to 56, and an ethylene oxide content of 60 to 85 mol %, based on the total amount of oxyalkylene groups present.
15. The composition as claimed in claim 13 , wherein the alkali metal salts of weak inorganic acids B) are selected from the group consisting of sodium hydroxide, sodium bicarbonate and sodium carbonate.
16. The composition as claimed in claim 13 wherein the components A) to H) are present in the composition in the following amounts:
A) 100 parts by weight of isocyanate-functional prepolymers,
B) 0.01 to 5 parts by weight of alkali metal salts of weak inorganic acids,
C) 0.1 to 200 parts by weight of water,
D) up to 100 parts by weight of heterocyclic oligomers,
E) 0 to 1 part by weight of catalysts,
F) 0 to 10 parts by weight of surfactants,
G) 0 to 20 parts by weight of mono- or polyhydric alcohols, and
H) up to 60 parts by weight of hydrophilic polyisocyanates.
17. A polyurethane foam obtained by the process as claimed in claim 1 .
18. A primary wound dressing, a cosmetic article or an incontinence product comprising the polyurethane foam as claimed in claim 17 .Cited by (0)
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